CARDIOMAX Defibrillator - Indonesia BPOM Medical Device Registration
CARDIOMAX Defibrillator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20505701622. The device is manufactured by INSTRAMED INDUSTRIA MEDICO HOSPITALAR LTDA. from Brazil, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ALKESTRON SELF-SOURCE.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
INSTRAMED INDUSTRIA MEDICO HOSPITALAR LTDA.Country of Origin
Brazil
Authorized Representative
PT. ALKESTRON SELF-SOURCEAR Address
Komplek Ruko Griya Inti Sentosa, JI. Griya Agung Blok O No.95, RT.2/RW.20
Registration Date
Mar 22, 2024
Expiry Date
Mar 14, 2029
Product Type
Therapeutic Cardiology Equipment
DC-defribrillator (including paddles)
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